Lei Zhang

发表

Changes in CT manifestations of patients with mild to moderate coronavirus disease 2019 in a Fangcang Shelter Hospital

W. Pu, Haijun Deng, Yang Wang, 2020 .

Down-regulation of EBAF in the heart with ventricular septal defects and its regulation by histone acetyltransferase p300 and transcription factors smad2 and cited2.

Xu Ma, D. Su, Qian Li, 2013, Biochimica et biophysica acta.

Comprehensive LRRK2 and GBA screening in Portuguese patients with Parkinson's disease: identification of a new family with the LRRK2 p.Arg1441His mutation and novel missense variants.

B. Oostra, J. Ferreira, M. Coelho, 2013, Parkinsonism & related disorders.

Compound heterozygote mutations in SPG7 in a family with adult-onset primary lateral sclerosis

K. Ahmeti, N. Siddique, T. Siddique, 2016, Neurology: Genetics.

Novel deletion and 2397 G>T mutations of the EXT1 gene identified in two Chinese pedigrees with hereditary multiple exostoses using exon sequencing

Lei Zhang, Liang-chao Dong, Yicheng Wang, 2020, Translational pediatrics.

Identification of novel compound heterozygous SPG7 mutations-related hereditary spastic paraplegia in a Chinese family: a case report

Gang Li, Yuanpeng Xia, Yanqing Wu, 2018, BMC Neurology.

Identification and Functional Analysis of GJA8 Mutation in a Chinese Family with Autosomal Dominant Perinuclear Cataracts

Lei Zhang, Xu Ma, Zhenfei Yang, 2013, PloS one.

Analysis of EXT 1 gene mutation in hereditary multiple exostosis families

Lei Zhang, Yang Shen, Feng Xie, 2016 .